Device recall
Z-0856-2009: RoboCouch Patient Support System, a component of the CyberKnife Robotic…
FDA device recall · Class II · Accuray Inc
Key facts
| Recall number (Z-number) | Z-0856-2009 |
|---|---|
| Recall event | 50208 |
| Product | RoboCouch Patient Support System, a component of the CyberKnife Robotic Radiosurgery System. Model number 025007, manufactured by Accuray Inc., Sunnyvale, CA The CyberKnife is indicated for treatment planning and imageguided stereotactic radiosurgery and precision radiotherapy of lesions, tumors and… |
| Product code | JAI |
| Recalling firm | Accuray Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 10, 2009 |
| 510(k) numbers | K042146 |
| FEI number | 1000123585 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database